bioRxivImmunologyPreprint
Immunological characterization of peritoneal exudate cells in liver cirrhosis patients
Shiori Kaji, Izumi SasakiiD, Satoko Kunimoto, Naoko Wakaki-Nishiyama, Emi Tosuji, Ayano Kurara, Takashi KatoiD, Chisako Mutsukawa, Daisuke OkuzakiiD, Chizuyo Okamoto, Yukiko Yamano, Ryo ShimizuiD, Shuya MaeshimaiD, Yoshiyuki IdaiD, Yasunobu YamashitaiD, Tadamichi Hashimoto, Sadahiro IwabuchiiD, Shinichi HashimotoiD, Shin-ichiroh SaitohiD, Shin‐ichi ArakiiD, Masayuki KitanoiD, Tsuneyasu KaishoiD
Abstract
BACKGROUND AND AIMSLiver cirrhosis (LC) is the end stage of liver fibrosis caused by various chronic liver diseases. Patients with LC often develop ascites containing peritoneal exudate cells (PECs). However, those cells have not been fully immunologically characterized. In this study, we clarify immune cell profiles of PECs from patients with LC. APPROACH AND RESULTSPECs were collected from patients with LC or patients receiving continuous ambulatory peritoneal dialysis (CAPD) as a non-cirrhotic control and subjected to single-cell RNA sequencing (scRNA-seq), bulk RNA sequencing (RNA-seq) and flowcytometry analyses. Analysis of scRNA-seq revealed that dendritic cells (DCs) and macrophages were major populations in CAPD patient-derived PECs, while those cells were decreased and T cells were most abundant in LC patient-derived PECs. Notably, FCGR3A-expressing macrophages were dominant over DCs and GATA6-expressing macrophages in LC patient-derived PECs. Bulk RNA-seq analysis further clarified expression of a set of genes was up- or down-regulated along with LC severity. Especially, expression of T cell signature genes was featured by its increase at Child-Pugh class B, but decrease at Child-Pugh class C. Flowcytometry analysis showed increase of T cells, decrease of DCs and macrophages, and increased expression of CD16 and CD163 in CD1cintCD14high cells corresponding to FCGR3A-expressing macrophages in LC patient-derived PECs. CONCLUSIONSIn LC patient-derived PECs, myeloid and T cell populations and their gene expression profiles were fluctuated with severity. Our findings should contribute to further development of diagnosis or therapeutic maneuver for LC.
- organism: human
- assay: scRNA-seq
- assay: bulk RNA-seq
- assay: flow cytometry
- research focus: cell type annotation
- research focus: differential expression
- approach: experimental assay
- Citations
- 1
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